A Copper-Catalyzed Reductive Defluorination of β-Trifluoromethylated

(1c,2k−m) Furthermore, in recent decades, the addition of nucleophiles to α-trifluoromethyl alkenes and subsequent β-fluoride elimination via an S...
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Letter Cite This: Org. Lett. 2018, 20, 1638−1642

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A Copper-Catalyzed Reductive Defluorination of β‑Trifluoromethylated Enones via Oxidative Homocoupling of Grignard Reagents Xiaoting Wu,† Fang Xie,*,† Ilya D. Gridnev,‡ and Wanbin Zhang*,† †

Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, P. R. China ‡ Department of Chemistry, Graduate School of Science, Tohoku University, Sendai 980-8578, Japan S Supporting Information *

ABSTRACT: An efficient copper-catalyzed reductive defluorination of β-trifluoromethylated enones via an oxidative homocoupling of Grignard reagents is reported. The reaction proceeded smoothly with a wide range of substrates, including the ones bearing aromatic heterocycles, such as furyl and thienyl ring systems in high yields (80−92%, except one example) under mild conditions. This provides a practical method for synthesis of gem-difluoroolefin ketones. It is also worth noting that this homocoupling process of Grignard reagents using β-trifluoromethylated enones as “oxidizing reagents” is effective for both the Csp2−Csp2 and Csp3−Csp3 bond formations, including for substrates whose β-hydride elimination of the corresponding transition metal alkyl complex is particularly facile, affording coupling products with high yields (83−95%), simultaneously.

Scheme 1. Cleavage of C−F Bond in the Trifluoromethyl Group Attached to a π Electron System under Electroreductive Conditions

gem-Difluoroalkenes are versatile building blocks in organic synthesis, in which the gem-difluorovinyl group can be transformed into various functionalities.1 Therefore, gemdifluoroalkene compounds have attracted significant interest and have become very important synthetic targets in academia and industry.1c,2 2-Trifluoromethyl-1-alkenes are reactive compounds, and their selective defluorination is a promising method for the preparation of difluoro compounds due to the availability of trifluoromethylated compounds.1c,2k−m Furthermore, in recent decades, the addition of nucleophiles to αtrifluoromethyl alkenes and subsequent β-fluoride elimination via an SN2′ reaction has been extensively explored, allowing for rapid access to gem-difluoroalkenes.2k,3 For SN2′ reactions of organic fluorides, metaphorically, an electron can be regarded as the smallest nucleophile. In general, it is not easy to cleave a C−F bond due to its strong bond energy. However, a C−F bond of the trifluoromethyl group that is attached to a π system can be readily cleaved under electroreductive conditions, since electron acceptance into the π-system and subsequent extrusion of a fluoride ion contribute greatly to the driving force of the reaction. However, to date, only a few reductive-type defluorinations for the preparation of gem-difluorovinyl groups have been reported, and they mostly consist of electrochemical reductions,4 the use of reductive metal magnesium,5 and photocatalytic conditions2m,6 (Scheme 1, previous work). As is well-known, oxidative homocoupling reactions of organometallic reagents occur with an oxidant; the oxidant can be regarded as an electron acceptor. Inspired by the mechanism of oxidative coupling reactions of organometallic reagents,7 we envisioned that an oxidative coupling reaction © 2018 American Chemical Society

may provide a convenient electron source and that compounds bearing a CF3 group attached to a π-system may accept electrons and thus act as an “oxidizing reagent”. This strategy provides a convenient electron source, which results in a reductive-type reaction of the trifluoromethyl group bonded to a π-electron system. gem-Difluoroalkenes are thus obtained Received: February 2, 2018 Published: March 7, 2018 1638

DOI: 10.1021/acs.orglett.8b00379 Org. Lett. 2018, 20, 1638−1642

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Organic Letters

used as a ligand of Cu(I)TC, and the yields of 2a and 3a (88% and 89%, respectively) increased (entry 3). Following screening of the copper salts and the amount of catalyst (entries 4−8), 1.0 mol % of Cu(I)TC was found to give the best result. The yields of 2a and 3a were further improved to 91% and 93%, respectively, and only a small quantity of 1,2-addition product (2a:4 = 91:9) was observed (entry 7). With the optimized reaction conditions (Table 1, entry 7) in hand, the scope of substrates 1 was then examined (Table 2).

accompanied by an oxidative homocoupling reaction of organometallic reagents (Scheme 1, our strategy). gem-Difluoroolefin ketones are versatile synthons for many fluorinated compounds and possess unique reactivity toward intramolecular SNV reactions.8 However, only two methodologies have been developed for their preparation: one required precious metal iridium as the catalyst via a photocatalytic decarboxylative/defluorinative reaction,6a and another required harsh reaction conditions and utilized hazardous and expensive reagents.9 On the other hand, homocoupling reactions of Grignard reagents allow for easy and efficient access to symmetrical compounds, and homocoupling reactions of aryl and alkenyl Grignard reagents have been extensively explored;10 however, the oxidative homocoupling of alkyl Grignard reagents,11,12 especially those bearing β-hydrogens,12 remains a challenge due to the difficulty of alkyl−alkyl couplings using transition metal catalysts. As part of our project on the Cu-catalyzed functionalization of enones,13 herein, we report a highly efficient synthesis of gemdifluoroolefin ketones via a copper-catalyzed reductive defluorination. Simultaneously, symmetrical biaryls, alkenes, and alkanes can be obtained effectively via oxidative homocoupling of Grignard reagents. In particular, this coupling process is also effective for Csp3−Csp3 bond formations (Scheme 1, this work). We began our study using β-trifluoromethylated enone 1a as a model substrate (Table 1), which can be readily obtained in

Table 2. Substrates Scope of β-Trifluoromethylated Enonesa

Table 1. Optimization of the Reaction Conditionsa

yield (%)c entry

ligand

CuX (mol %)

1 2 3 4 5 6 7 8

− − PPh3 PPh3 PPh3 PPh3 PPh3 PPh3

− Cu(I)TC (2.5) Cu(I)TC (2.5) Cu(I)I (2.5) Cu(II)(OAc)2 (2.5) Cu(II)Br2 (2.5) Cu(I)TC (1.0) Cu(I)TC (0.1)

2a:4

b

b

4:96 69:31 90:10 83:17 75:25 77:23 91:9 81:19

2a trace 66 88 81 73 74 91 80

3a b

traceb 65 89 81 77 76 93 82

a The reaction of 1a (0.20 mmol) with PhMgBr (2.5 equiv) was performed in DCM (2.0 mL) at room temperature for 3 h in the presence of the complex in situ from CuX (n mol %) and PPh3 (2n mol %). bDetermined by 1H NMR spectroscopy. cYield of products isolated after chromatography.

a

The reaction of 1a−x (0.50 mmol) with PhMgBr (2.5 equiv) was performed in DCM (5.0 mL) at room temperature for 3 h in the presence of the complex formed in situ from Cu(I)TC (0.005 mmol, 1.0 mol %) and PPh3 (0.01 mmol, 2.0 mol %). bYield of products (2a−x) and product 3a isolated after chromatography.

high yield by the reaction of commercially available trifluoroacetophenone and a Wittig reagent.14 A blank experiment using 1a with PhMgBr in the absence of a copper salt provided 1,2addition product 4 as the major product (entry 1). Under our assumption above (Scheme 1), the reaction was carried out by employing PhMgBr and Cu(I)TC (copper(I)-thiophene-2carboxylate) in the presence of 1a in DCM and at room temperature over 3 h. To our delight, the gem-difluoroolefins ketone 2a and biphenyl 3a products were obtained in yields of 66% and 65%, respectively, accompanied by a minor 1,2addition product 4 (2a:4 = 69:31) (entry 2). Next, PPh3 was

The reaction proceeded smoothly with a wide range of substrates. The influence of the R1 group in substrates 1 was first investigated. When R1 was an alkyl group, such as Et or Cy, the desired products (2b−c) were afforded in moderate to good yields (66% and 81%, respectively). When R1 was either a phenyl or substituted phenyl group, good to high yields (80− 92%) of the corresponding gem-difluoroolefins ketones (2a, 1639

DOI: 10.1021/acs.orglett.8b00379 Org. Lett. 2018, 20, 1638−1642

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smoothly, with the coupling also being highly stereoselective. Of particular note is that the Csp3−Csp3 homocoupling products (3l−3o) were obtained in good yields (83−92%) including those from reactions with PhCH(CH3)MgBr, Ph(CH2)2MgBr, and Ph(CH2)3MgBr (3m, 83%; 3n, 92%; 3o, 91%). These three substrates are especially challenging since β-hydride elimination of the corresponding transition metal alkyl complex is particularly facile. Notably, the homocoupling product of PhCH(CH3)MgBr is only meso-2,3diphenylbutane (3m) with none of the D,L-2,3-diphenylbutane being observed. We next turned our attention to the reaction mechanism. According to a blank experiment (Table 1, entry 1), the major product was 1,2-addition product 4, with only trace amounts of 2a and 3a being observed in the absence of the copper salt under the optimized reaction conditions (Table 1, entry 7), which indicated that this reaction required a copper catalyst. Furthermore, when 2.0 equiv of TEMPO were used as a radical scavenger in this reaction system (see Supporting Information), 2a and 3a were isolated in yields of 90% and 92%, respectively, yields that are identical to those obtained in the absence of TEMPO. This result suggests that the reaction does not proceed through a radical process. On the basis of the experimental results and previous reports,4,7 a possible catalytic pathway for the reaction of 1a with PhMgBr has been proposed (Scheme 2). The reaction process may begin with an

2d−q) were obtained, irrespective of the electronic properties or substitution pattern on the aromatic ring. In addition, the reaction scope was expanded to include substrates bearing aromatic heterocycles, such as furyl and thienyl ring systems. The desired products (2r−s) were obtained with excellent yields (91% and 92%, respectively). With R2 being a substituted phenyl group bearing electron-rich or electron-poor substituents, the reactions proceeded well to afford the corresponding gem-difluoroolefins ketones (2t−w) in high yields (85−91%). Finally, β-CF3-α,β,γ,δ-dienone (1x) was also employed as a substrate in this reaction, giving the corresponding product (4E)-2x in 89% yield. Additionally, it is also worth noting that the oxidative homocoupling product 3a of PhMgBr provided similarly high yields using this Cu-catalyzed reductive-type reaction of trifluoromethyl groups bonded to a π-electron system. This suggests that the Cu-catalyzed system could also be of use for the oxidative homocoupling of Grignard reagents using 1 as an “oxidizing reagent”, a reaction which has not been previously reported. Subsequently, the scope of Grignard reagents in the reaction with 1a was investigated (Table 3). First, various Table 3. Substrates Scope of Grignard Reagentsa

Scheme 2. Proposed Reaction Mechanism

organocopper reagent PhCu(I), which formed via transmetalation of PhMgBr and Cu(I)TC. Treatment with another equivalent of PhMgBr results in the formation of a copper monoanionic salt A.7a,b Subsequent oxidative homocoupling with 1a acting as an oxidant, electron acceptance into the πsystem of 1a, and extrusion of a fluoride ion afford biphenyl 3a and the copper species B. The copper species B is readily transmetalated with another equivalent of PhMgBr to provide the magnesium species C, which is hydrolyzed to form the target product 2a. The organocopper reagent PhCu(I) is regenerated to complete the catalytic cycle. To further demonstrate the utility of our methodology for the synthesis of gem-difluoroolefin ketones, a gram-scale reaction was conducted, and gem-difluoroolefin ketone 2a and biphenyl 3a were obtained in 88% and 89% yields, respectively (Scheme 3a). In addition, MeMgBr and EtMgBr were used in place of PhMgBr, and 2a was obtained easily in high yields (92% and 90%, respectively), accompanied by the formation of

a The reaction of 1a (0.50 mmol) with RMgBr (2.5 equiv) was performed in DCM (5.0 mL) at room temperature for 3 h in the presence of the complex in situ from Cu(I)TC (0.005 mmol, 1.0 mol %) and PPh3 (0.01 mmol, 2.0 mol %). bYield of products (3a−o) and product 2a isolated after chromatography.

substituted aryl magnesium reagents were coupled in high yields (90−95%). Functional groups, such as alkyl (3b), alkoxy (3c, 3f−h), fluorine (3d), and trifluoromethyl (3e), were all well tolerated, irrespective of the substitution pattern on the aromatic ring. 1- or 2-Naphthylmagnesium reagents were also amenable to this reaction and afforded their corresponding binaphthyls 3i and 3j with high yields (94% and 95%, respectively). A phenyl substituted alkenyl Grignard reagent also afforded its corresponding conjugated diene (3k) 1640

DOI: 10.1021/acs.orglett.8b00379 Org. Lett. 2018, 20, 1638−1642

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Scheme 3. Gram-Scale Reactions of 1a

Letter

ASSOCIATED CONTENT

S Supporting Information *

The Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/acs.orglett.8b00379. Experimental procedures and characterization data for all reactions and products, including 1H, 13C, and 19F NMR spectra (PDF)



ethane or butane, which are readily expelled as gas from the reaction mixture (Scheme 3b). To test the versatility of gem-difluoroolefin ketones obtained via the aforementioned sequence, we performed several transformations on γ,γ-difluoroallylic ketone 2a (Scheme 4).

AUTHOR INFORMATION

Corresponding Authors

*[email protected]. *[email protected]. ORCID

Scheme 4. Conversions of γ,γ-Difluoroallylic Ketone 2a

Wanbin Zhang: 0000-0002-4788-4195 Notes

The authors declare no competing financial interest.



ACKNOWLEDGMENTS We thank the NSFC (Nos. 21572129 and 21620102003) and Shanghai Municipal Education Commission (No. 201701070002E00030).



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The product 2a can be readily converted to the corresponding γ,γ-difluoro allylic alcohol 5 in a yield of 99% by addition of PhMgBr. Fortunately, 5 can be readily converted to 2fluorinated dihydrofuran 6 in a yield of 95% via an intramolecular SNV reaction, thus averting tedious syntheses of fluorine-containing five-membered heterocycles, which usually require harsh reaction conditions.2d,8,15 In addition, the corresponding gem-difluorodiene 7 was obtained in 99% yield via a dehydration reaction of 5. Interestingly, hydrogenation of compound 2a with H2 in the presence of a Pd/C catalyst and in different solvents allowed for the selective formation of the hydrogenated products in high yields (8, 99%; 9, 99%). In addition, 2a can also be converted to tetrasubstituted 2H-pyrrole 10 in a yield of 92% by reaction with benzyl amine in the presence of a ZnCl2 catalyst. In conclusion, we have developed an efficient synthesis of gem-difluoroolefin ketones via a copper-catalyzed reductive defluorination, accompanying an oxidative homocoupling of Grignard reagents for the synthesis of symmetrical alkanes or biaryls. This reaction can be performed under mild conditions providing high yields for the two desired products, simultaneously. In particular, this coupling process is effective for Csp3−Csp3 bond formation, including for substrates whose βhydride elimination of the corresponding transition metal alkyl complex is particularly facile. 1641

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